Ultrastructural observations on the cells of a patient with Fanconi's anemia transforming to acute leukemia.

R Straussberg, H Bessler, S Alexandrova, H Salman, M Bergman, M Djaldetti
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Abstract

The ultrastructural findings in the bone marrow and peripheral blood cells of a patient with Fanconi's anemia transforming to acute myelo-monocytic leukemia are presented. They consisted of an unusual large number of nuclear pockets, bridges and appendices observed in the nuclei of the polymorphonuclear cells, monocytes and to a lesser extent in the mature normoblasts. Since the mother and two younger brothers of the propositus were found to have macrocytic anemia and pancytopenia, most probably Fanconi's anemia, their peripheral blood cells were also examined with the electron microscope. The cells of all of them showed similar nuclear alterations, although in lesser quantity. The possibility that these findings are consistent with the diagnosis of Fanconi's anemia, or they herald an evolution of the disease to acute leukemia is considered.

范可尼贫血转化为急性白血病的细胞超微结构观察。
本文报道一例范可尼贫血转化为急性髓单核细胞白血病的患者骨髓和外周血细胞超微结构的变化。在多形核细胞、单核细胞的细胞核中观察到异常多的核袋、核桥和核附件,在成熟的正母细胞中也有少量观察到。由于母亲和两个弟弟被发现患有巨细胞性贫血和全血细胞减少症,很可能是范可尼贫血,他们的外周血也被电子显微镜检查了。所有的细胞都表现出类似的细胞核改变,尽管数量较少。这些发现可能与范可尼贫血的诊断一致,或者它们预示着该疾病向急性白血病的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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